NDC 0023-3921 – Botox

Botulinum Toxin Type A 200 [USP'U]/1 · Injection, Powder, Lyophilized, For Solution · Intradermal, Intramuscular

Human Prescription Drug

Product NDC0023-3921

Product details

Brand name
Botox
Generic name
onabotulinumtoxinA
Labeler
Allergan, Inc.
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intradermal, Intramuscular
Marketing category
BLA · BLA103000
Marketed since
January 11, 2010
Listing expires
December 31, 2027
Pharmacologic class
Acetylcholine Release Inhibitor; Neuromuscular Blocker

Active ingredients

Uses, dosage, side effects and warnings for Botox →

Package NDC codes (2)

Package NDCDescriptionSince
0023-3921-021 VIAL in 1 CARTON (0023-3921-02) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIALJan 11, 2010
0023-3921-03 sample1 VIAL in 1 CARTON (0023-3921-03) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIALJan 11, 2010

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